Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Carolin Meyerhoff"'
Autor:
Anna Reustle, Moreno Di Marco, Carolin Meyerhoff, Annika Nelde, Juliane S. Walz, Stefan Winter, Siahei Kandabarau, Florian Büttner, Mathias Haag, Linus Backert, Daniel J. Kowalewski, Steffen Rausch, Jörg Hennenlotter, Viktoria Stühler, Marcus Scharpf, Falko Fend, Arnulf Stenzl, Hans-Georg Rammensee, Jens Bedke, Stefan Stevanović, Matthias Schwab, Elke Schaeffeler
Publikováno v:
Genome Medicine, Vol 12, Iss 1, Pp 1-24 (2020)
Abstract Background Clear cell renal cell carcinoma (ccRCC) is the dominant subtype of renal cancer. With currently available therapies, cure of advanced and metastatic ccRCC is achieved only in rare cases. Here, we developed a workflow integrating d
Externí odkaz:
https://doaj.org/article/fc55be784afc4fe685c251765eeb65fb
Autor:
Anna Reustle, Moreno Di Marco, Carolin Meyerhoff, Annika Nelde, Juliane S. Walz, Stefan Winter, Siahei Kandabarau, Florian Büttner, Mathias Haag, Linus Backert, Daniel J. Kowalewski, Steffen Rausch, Jörg Hennenlotter, Viktoria Stühler, Marcus Scharpf, Falko Fend, Arnulf Stenzl, Hans-Georg Rammensee, Jens Bedke, Stefan Stevanović, Matthias Schwab, Elke Schaeffeler
Publikováno v:
Genome Medicine
Genome Medicine, Vol 12, Iss 1, Pp 1-24 (2020)
Genome Medicine, Vol 12, Iss 1, Pp 1-24 (2020)
Background Clear cell renal cell carcinoma (ccRCC) is the dominant subtype of renal cancer. With currently available therapies, cure of advanced and metastatic ccRCC is achieved only in rare cases. Here, we developed a workflow integrating different
Autor:
Florian Büttner, Carolin Meyerhoff, Siarhei Kandabarau, Stefan Winter, Steffen Rausch, Arnulf Stenzl, Falko Fend, Christopher Schroeder, Peter Bauer, Per Hoffmann, Markus M. Nöthen, Jens Bedke, Matthias Schwab, Elke Schaeffeler
Publikováno v:
Cancer Research. 79:2529-2529
Renal cell carcinoma (RCC) accounts for 5% in men and 3% in women of all oncological diagnoses worldwide (Capitanio et al., Eur Urol 2018). In 0.7-4.7% of patients both kidneys are affected by cancer. Although hereditary forms of RCC do exist (VHL di